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		<title><![CDATA[discussion boards — Mets to bones]]></title>
		<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?id=280</link>
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		<description><![CDATA[The most recent posts in Mets to bones.]]></description>
		<lastBuildDate>Wed, 22 Nov 2006 20:19:25 +0000</lastBuildDate>
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			<title><![CDATA[Re: Mets to bones]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1226#p1226</link>
			<description><![CDATA[<p>I think Caroline Stoufer has mets to the bones.&nbsp; Check out her blog.</p>]]></description>
			<author><![CDATA[null@example.com (Sara)]]></author>
			<pubDate>Wed, 22 Nov 2006 20:19:25 +0000</pubDate>
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			<title><![CDATA[Mets to bones]]></title>
			<link>http://www.cholangiocarcinoma.org/punbb/viewtopic.php?pid=1224#p1224</link>
			<description><![CDATA[<p>Hi Everyone,<br />Just an update on my husband.&nbsp; Just after 4 months of no treatment and no signs of cancer, a bone scan shows mets to pelvis as well as 4 small lesions in the liver.&nbsp; To say the least this has been very disappointing news.&nbsp; We have not seen the oncologist yet, this news is from a radiologist report so we are not sure what this means in terms of treatment.&nbsp; His previous treatment was oxilyplatin and gemcitibine, 5 FU and radiation.&nbsp; He absolutely dreads the idea of beginning treatment again although I can&#039;t believe it will ever be a rough as the first go round.&nbsp; &nbsp;He still suffers from neuropathy in his hands and feet.&nbsp; &nbsp;Has anyone had a similar experience with mets to the bone?&nbsp; He already had radiation to the liver.&nbsp; Can you max out on the amount of radiation to the body?&nbsp; Trying to get prepared for what to expect.&nbsp; Thanks .&nbsp; Happy Thanksgiving!<br />Joyce</p>]]></description>
			<author><![CDATA[null@example.com (jberg597)]]></author>
			<pubDate>Wed, 22 Nov 2006 17:59:07 +0000</pubDate>
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